SCHEMBL410747

SCHEMBL410747

O=[N+]([O-])c1ccccc1S(=O)(=O)Nc1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AR P10275 1/20 0.67
GAA P10253 1/20 0.67
SMN1; SMN2 Q16637 1/20 0.67
CA2 P00918 2/20 0.65
CA1 P00915 1/20 0.65
MMP1 P03956 1/20 0.65
MMP2 P08253 1/20 0.65
MMP9 P14780 1/20 0.65
MMP8 P22894 1/20 0.65
MMP13 P45452 1/20 0.65
L3MBTL1 Q9Y468 1/20 0.64
KMT2A Q03164 4/20 0.59
MEN1 O00255 3/20 0.59
CA12 O43570 1/20 0.58
CA9 Q16790 1/20 0.58
PKM P14618 2/20 0.58
HTT P42858 1/20 0.56
HSPD1 P10809 1/20 0.55
PTPN2 P17706 1/20 0.55
PTPN1 P18031 1/20 0.55

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL31235173 1.00 AR (0.67) ARGAASMN1; SMN2CA2CA1
SCHEMBL95754 0.89 GAA (0.66) ARGAASMN1; SMN2CA2CA1
SCHEMBL641243 0.87 SMN1; SMN2 (0.64) ARGAASMN1; SMN2CA2CA1
SCHEMBL7445075 0.87 GAA (0.64) ARGAASMN1; SMN2CA2CA1
SCHEMBL2452111 0.87 GAA (0.64) ARGAASMN1; SMN2CA2CA1
SCHEMBL3917522 0.84 AR (0.67) ARGAASMN1; SMN2CA2CA1
SCHEMBL3625980 0.84 L3MBTL1 (0.69) ARGAASMN1; SMN2CA2CA1
SCHEMBL17077916 0.84 L3MBTL1 (0.65) ARGAASMN1; SMN2CA2CA1
SCHEMBL1575942 0.84 GAA (0.64) ARGAASMN1; SMN2CA2CA1
SCHEMBL28270283 0.84 L3MBTL1 (0.65) ARGAASMN1; SMN2CA2CA1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 75 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116836130-B Synthesis method of 3, 4-dihydrobenzothiadiazine compound 嘉实(湖南)医药科技有限公司 2023-11-21 CN disclosed
EP-4276092-A1 COMPOUND LIBRARY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-11-15 EP disclosed
CN-116836130-A Synthesis method of 3, 4-dihydrobenzothiadiazine compound 嘉实(湖南)医药科技有限公司 2023-10-03 CN disclosed
CN-116783160-A Libraries of compounds 中外制药株式会社 2023-09-19 CN disclosed
US-10183011-B2 Anti-depression compounds BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2019-01-22 US disclosed
US-10172827-B2 Pro-neurogenic compounds BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2019-01-08 US disclosed
US-20180318255-A1 Pro-Neurogenic Compounds BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM 2018-11-08 US disclosed
EP-2385829-B1 PRO-NEUROGENIC COMPOUNDS UNIV TEXAS (US) 2018-08-01 EP disclosed
US-20180127367-A1 Pro-Neurogenic Compounds NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2018-05-10 US disclosed
US-9962368-B2 Pro-neurogenic compounds BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 2018-05-08 US disclosed
US-6967196-B1 Sulfonamide compounds and uses thereof BRISTOL-MYERS SQUIBB COMPANY (US) 2005-11-22 US disclosed
CN-1349381-A Sulfonamide derivatives TAKEDA CHEMICAL INDUSTRIES LTD (JP) 2002-05-15 CN disclosed
US-5783699-A MAY BE CONJUGATED TO ANTIGENS, HAPTENS, ANTIBODIES IN IMMUNOASSAYS ABBOTT LABORATORIES (US) 1998-07-21 US disclosed
US-5669819-A IMMUNOASSAY ABBOTT LABORATORIES (US) 1997-09-23 US disclosed
US-5565570-A REACTING AMINE WITH SULFONYL HALIDE IN INERT SOLVENT IN PRESENCE OF BASE TO FORM METAL SALT OF SULFONAMIDE, ACYLATING WITH ACTIVATED PHENANTHRIDINE-6-CARBOXYLIC ACID TO FORM CHEMILUMINESCENT SALT ABBOTT LABORATORIES (US) 1996-10-15 US disclosed
US-5545739-A E.G., 5-METHYL-6-(N-2-CARBOXYETHYL-N=(2-CARBOXYETHYL)-PHENANTHRIDIN IUMCARBOXAMIDE CHLORIDE; IMMUNOASSAYS; STABILITY; SENSITIVITY ABBOTT LABORATORIES (US) 1996-08-13 US disclosed
US-5543524-A FORMING A SULFONAMIDE FROM AND AMINE AND A SULFONYL HALIDE AND AND ACYLATING WITH A CARBONYL HALIDE OF AN ACTIVATED ACRIDINE SALT ABBOTT LABORATORIES (US) 1996-08-06 US disclosed
US-5468646-A Chemiluminescent acridinium salts ABBOTT LABORATORIES (US) 1995-11-21 US disclosed
EP-0273115-B1 Chemiluminescent acridinium and phenanthridinium salts ABBOTT LAB (US) 1994-09-07 EP disclosed
US-4497828-A 3-Nitro-4-methylbenzene sulfon-2-chloro-4-nitroanilide and fungicidal composition for the control of plant diseases containing same MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1985-02-05 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10172827-B2 Pro-neurogenic compounds DCX, GAP43, BDNF AR 4203/4885GAA 3570/4885SMN1; SMN2 182/4885
US-20180127367-A1 Pro-Neurogenic Compounds BDNF, GAP43, DCX AR 3839/4885GAA 963/4885SMN1; SMN2 50/4885
US-20180318255-A1 Pro-Neurogenic Compounds BDNF, GAP43, DCX AR 3839/4885GAA 963/4885SMN1; SMN2 50/4885
US-10183011-B2 Anti-depression compounds BDNF, DCX, GAP43 AR 3858/4885GAA 763/4885SMN1; SMN2 63/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.